Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:82063994..82066273-chr3:82070206..82072122,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1529028	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4856206	0.90[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57027601	0.93[AFR][1000 genomes]
rs57551871	0.93[AFR][1000 genomes]
rs57996908	0.93[AFR][1000 genomes]
rs58087753	0.93[AFR][1000 genomes]
rs60957164	0.93[AFR][1000 genomes]
rs61484580	0.93[AFR][1000 genomes]
rs72895828	0.93[AFR][1000 genomes]
rs72895832	0.93[AFR][1000 genomes]
rs72895845	0.93[AFR][1000 genomes]
rs72895859	0.86[AFR][1000 genomes]
rs72897645	0.86[AFR][1000 genomes]
rs72897657	0.93[AFR][1000 genomes]
rs72897671	0.93[AFR][1000 genomes]
rs72897675	0.93[AFR][1000 genomes]
rs72897678	0.93[AFR][1000 genomes]
rs72897682	0.93[AFR][1000 genomes]
rs72897700	0.93[AFR][1000 genomes]
rs72899615	0.93[AFR][1000 genomes]
rs72899624	0.93[AFR][1000 genomes]
rs9811429	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007167	chr3:82050178-82301466	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82064000-82064400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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